Genotype–phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo-Reference-Cited by-同舟云学术

Genotype–phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo

Published:2020-07-19 Issue:1 Volume:191 Page:
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Bravo‐Pérez C.¹^ORCID,Morena‐Barrio M. E.¹^ORCID,Palomo A.²,Entrena L.³,Morena‐Barrio B.¹^ORCID,Padilla J.¹,Miñano A.¹,Navarro E.¹,Cifuentes R.¹,Corral J.¹,Vicente V.¹

Affiliation:

1. Servicio de Hematología y Oncología Médica Hospital Universitario Morales MeseguerCentro Regional de HemodonaciónUniversity of MurciaIMIB‐ArrixacaCIBERER MurciaSpain

2. Servicio de Hematología y Hemoterapia del centro Materno‐Infantil del Hospital Regional Universitario Carlos de Haya MálagaSpain

3. Servicio de Hematología Hospital Virgen de las Nieves Granada Spain

Funder

Instituto de Salud Carlos III

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.16963

Reference12 articles.

1. Structure of β-Antithrombin and the Effect of Glycosylation on Antithrombin's Heparin Affinity and Activity